Staff Manufacturing Engineer, NPI

Irvine, CA - USA

Monthly Salary: Not Disclosed

Posted on: 4 hours ago

Vacancies: 1 Vacancy

Job Summary

Work Flexibility: Onsite

Position summary

This position independently leads complex activities and tasks in support of manufacturing operations. Activities and tasks are conducted on materials products processes and equipment. Receives minimal direction /review and is viewed as an expert in one or more in-house technologies.

Key areas of responsibility

Independently lead complex activities to design document and improve manufacturing processes and operations that control the safety and efficacy of components or finished devices.
Independently lead qualification verification and validation activities for the production of components or medical devices.
Analyze troubleshoot and resolve issues relating to the safety efficacy quality cost or delivery of components and finished devices.
Drive complex engineering work new product development teams and product support typically including the following activities: technology development test of materials or products preparation of specifications Six Sigma process study process improvements and report preparation. Work is expected to broaden Strykers Intellectual Property in strategic areas.
Drive the design & development of manufacturing equipment in compliance with manufacturing safety (e.g. OSHA & EPA) principles.
Participate in design control efforts related to risk analysis (FMEA) & design reviews.
Preferred: Source component and service suppliers; assess supplier capability and effectiveness.
Lead efforts related to design maintenance and troubleshooting of controlled environment (facilities & equipment).
Train mentor and provide work direction to operators technicians and engineers.
Functional participant in post-market surveillance & annual product performance reviews.
Lead in the identification implementation and management of production goals.
Lead complex cross-functional project teams. Coordinate manage and document project goals and progress and recommend appropriate revisions.
Design and coordinate complex engineering tests and experiments. Analyze data draw conclusions and summarize test results. Communicate results to the technical community.
Interfaces with product builders or extrusion technicians production supervisors and engineers in troubleshooting problems on the production floor.
Participates in project teams typically including one of the following:
Identifying and implementing process/product improvement alternatives to increase/optimize yield efficiency throughput and/or performance.
Designing performing and documenting engineering test experiments to evaluate product/process performance.
Designing developing testing and validating equipment and processes; analyzing and interpreting process models and recommending process improvements.
Evaluating external process technologies.
Identify and implement projects for cost savings.
Influence decisions around alternative engineering processes products and equipment.
Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.

Minimum Requirements:

Four-year engineering degree or a technical discipline. MS CQE or CRE preferred.
4 or more years experience in manufacturing engineering

Preferred Skills:

2 years medical products experience
Ability to conduct complex statistical geometric and mathematical calculations.
Ability to read understand create engineering drawings on common engineering software.
Proficient in use of Minitab or similar statistical and Microsoft Office software
Demonstrate a primary commitment to patient safety product quality and compliance with the Stryker Quality Manual and its governing regulations.
Demonstrated ability in forward looking perspective in relation to capacity & cost-control issues.
Demonstrated ability to effectively write and review technical documents & investigative reports.
Ability to mentor Engineers and other technical staff.

Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.

Required Experience:

Staff IC

Work Flexibility: OnsitePosition summaryThis position independently leads complex activities and tasks in support of manufacturing operations. Activities and tasks are conducted on materials products processes and equipment. Receives minimal direction /review and is viewed as an expert in one or mor...

Work Flexibility: Onsite

Position summary

Key areas of responsibility

Independently lead complex activities to design document and improve manufacturing processes and operations that control the safety and efficacy of components or finished devices.
Independently lead qualification verification and validation activities for the production of components or medical devices.
Analyze troubleshoot and resolve issues relating to the safety efficacy quality cost or delivery of components and finished devices.
Drive complex engineering work new product development teams and product support typically including the following activities: technology development test of materials or products preparation of specifications Six Sigma process study process improvements and report preparation. Work is expected to broaden Strykers Intellectual Property in strategic areas.
Drive the design & development of manufacturing equipment in compliance with manufacturing safety (e.g. OSHA & EPA) principles.
Participate in design control efforts related to risk analysis (FMEA) & design reviews.
Preferred: Source component and service suppliers; assess supplier capability and effectiveness.
Lead efforts related to design maintenance and troubleshooting of controlled environment (facilities & equipment).
Train mentor and provide work direction to operators technicians and engineers.
Functional participant in post-market surveillance & annual product performance reviews.
Lead in the identification implementation and management of production goals.
Lead complex cross-functional project teams. Coordinate manage and document project goals and progress and recommend appropriate revisions.
Design and coordinate complex engineering tests and experiments. Analyze data draw conclusions and summarize test results. Communicate results to the technical community.
Interfaces with product builders or extrusion technicians production supervisors and engineers in troubleshooting problems on the production floor.
Participates in project teams typically including one of the following:
Identifying and implementing process/product improvement alternatives to increase/optimize yield efficiency throughput and/or performance.
Designing performing and documenting engineering test experiments to evaluate product/process performance.
Designing developing testing and validating equipment and processes; analyzing and interpreting process models and recommending process improvements.
Evaluating external process technologies.
Identify and implement projects for cost savings.
Influence decisions around alternative engineering processes products and equipment.
Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.

Minimum Requirements:

Four-year engineering degree or a technical discipline. MS CQE or CRE preferred.
4 or more years experience in manufacturing engineering

Preferred Skills:

2 years medical products experience
Ability to conduct complex statistical geometric and mathematical calculations.
Ability to read understand create engineering drawings on common engineering software.
Proficient in use of Minitab or similar statistical and Microsoft Office software
Demonstrate a primary commitment to patient safety product quality and compliance with the Stryker Quality Manual and its governing regulations.
Demonstrated ability in forward looking perspective in relation to capacity & cost-control issues.
Demonstrated ability to effectively write and review technical documents & investigative reports.
Ability to mentor Engineers and other technical staff.

Travel Percentage: 10%

Required Experience:

Staff IC

Key Skills

Lean Manufacturing
Six Sigma
CNC Programming
Lean
Machining
Tooling
CAD
CNC
Assembly Experience
SolidWorks
Kaizen
Manufacturing

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About Company

Stryker

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongsid ... View more

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